Follistatin in chondrocytes: the link between TRPV4 channelopathies and skeletal malformations

Point mutations in the calcium-permeable TRPV4 ion channel have been identified as the cause of autosomal-dominant human motor neuropathies, arthropathies, and skeletal malformations of varying severity. The objective of this study was to determine the mechanism by which TRPV4 channelopathy mutation...

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Hlavní autoři: Leddy, Holly A., McNulty, Amy L., Lee, Suk Hee, Rothfusz, Nicole E., Gloss, Bernd, Kirby, Margaret L., Hutson, Mary R., Cohn, Daniel H., Guilak, Farshid, Liedtke, Wolfgang
Médium: Artigo
Jazyk:Inglês
Vydáno: Federation of American Societies for Experimental Biology 2014
Témata:
Research Communications
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC4021446/
https://ncbi.nlm.nih.gov/pubmed/24577120
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1096/fj.13-245936
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